Androgen Receptor (AR-V7 specific) Rabbit Monoclonal Antibody

Androgen Receptor (AR-V7 specific) Rabbit Monoclonal Antibody

Cat: AMRe87492
Size1:50μL Price1:$188
Size2:100μL Price2:$338
Application:WB, ICC/IF, FC

Reactivity:Human
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:Androgen Receptor (AR-V7 specific)
Category: Recombinant Monoclonal Antibody Tags: , , , , ,

Summary

Production Name

Androgen Receptor (AR-V7 specific) Rabbit Monoclonal Antibody

Description

Rabbit Monoclonal antibody

Host

Rabbit

Application

WB, ICC/IF, FC

Reactivity

Human

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

IgG

Clonality

Monoclonal Antibody

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein . Stable for 12 months from date of receipt.

Purification

Affinity Purification

 

Immunogen

Gene Name

Androgen Receptor (AR-V7 specific)

Alternative Names

KD; AIS; AR8; TFM; DHTR; SBMA; HYSP1; NR3C4; SMAX1; HUMARA

Gene ID

367

SwissProt ID

P10275-3

 

Application

Dilution Ratio

WB: 1:1000 ICC/IF: 1:50 FC: 1:20-1:50

Molecular Weight

Calculated MW:67 kDa; Observed MW:80 kDa

 

Background

The androgen receptor gene is more than 90 kb long and codes for a protein that has 3 major functional domains: the N-terminal domain, DNA-binding domain, and androgen-binding domain. The protein functions as a steroid-hormone activated transcription factor. Upon binding the hormone ligand, the receptor dissociates from accessory proteins, translocates into the nucleus, dimerizes, and then stimulates transcription of androgen responsive genes. This gene contains 2 polymorphic trinucleotide repeat segments that encode polyglutamine and polyglycine tracts in the N-terminal transactivation domain of its protein. Expansion of the polyglutamine tract from the normal 9-34 repeats to the pathogenic 38-62 repeats causes spinal bulbar muscular atrophy (SBMA, also known as Kennedy's disease). Mutations in this gene are also associated with complete androgen insensitivity (CAIS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2017]

 

Research Area